Natural Compounds and Organic Synthesis Laboratory, Migal-Galilee Research Institute, Kiryat Shmona 11016, Israel.
Department of Biotechnology, Tel-Hai Academic College, Kiryat Shmona 11016, Israel.
Int J Mol Sci. 2024 Sep 26;25(19):10344. doi: 10.3390/ijms251910344.
Chiral pincer complexes, characterized by their rigid tridentate coordination framework, have emerged as powerful catalysts in asymmetric synthesis. This review provides a comprehensive overview of recent advancements in the development of chiral pincer-type ligands and their corresponding transition metal complexes. We highlight the latest progress in their application across a range of catalytic asymmetric reactions, including the (transfer) hydrogenation of polar and non-polar bonds, hydrophosphination, alkynylation, Friedel-Crafts reactions, enantioselective reductive cyclization of alkynyl-tethered cyclohexadienones, enantioselective hydrosilylation, as well as Aza-Morita-Baylis-Hillman reactions. The structural rigidity and tunability of chiral pincer complexes enable precise control over stereoselectivity, resulting in high enantioselectivity and efficiency in complex molecular transformations. As the field advances, innovations in ligand design and the exploration of new metal centers are expected to expand the scope and utility of these catalysts, bearing significant implications for the synthesis of enantioenriched compounds in pharmaceuticals, materials science, and beyond.
手性钳状配合物以其刚性的三齿配位骨架为特征,已成为不对称合成中的有力催化剂。本综述全面概述了手性钳型配体及其相应过渡金属配合物的最新发展。我们重点介绍了它们在一系列催化不对称反应中的最新应用进展,包括极性和非极性键的(转移)氢化、膦氢化、炔基化、傅克反应、炔基连接的环己二烯酮的对映选择性还原环化、对映选择性硅氢化以及氮杂-Morita-Baylis-Hillman 反应。手性钳状配合物的结构刚性和可调节性能够精确控制立体选择性,从而在复杂分子转化中实现高对映选择性和效率。随着该领域的发展,配体设计的创新和新金属中心的探索有望扩大这些催化剂的范围和实用性,在手性化合物合成、材料科学等领域具有重要意义。